FDA inspection

Beijing Aeonmed Company Limited: FDA inspection ending Jul 18, 2019

FDA inspection 1099707 · Voluntary Action Indicated (VAI) · Langfang

Key facts

Inspection ID 1099707
Firm Beijing Aeonmed Company Limited
FEI number 3007238566
Address No. 10 Chaobai Street, Yingbin Road West, Yanjiao Development Zone
City Langfang
Country China
Fiscal year 2019
Inspection end date Jul 18, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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